JP2008189791A - Friction material - Google Patents
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- JP2008189791A JP2008189791A JP2007025128A JP2007025128A JP2008189791A JP 2008189791 A JP2008189791 A JP 2008189791A JP 2007025128 A JP2007025128 A JP 2007025128A JP 2007025128 A JP2007025128 A JP 2007025128A JP 2008189791 A JP2008189791 A JP 2008189791A
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- friction
- potassium titanate
- friction material
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- sulfide
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- 239000002783 friction material Substances 0.000 title claims abstract description 29
- 239000000463 material Substances 0.000 claims abstract description 24
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 claims abstract description 18
- ITRNXVSDJBHYNJ-UHFFFAOYSA-N tungsten disulfide Chemical compound S=[W]=S ITRNXVSDJBHYNJ-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000002994 raw material Substances 0.000 claims abstract description 13
- 239000000835 fiber Substances 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 9
- 239000011230 binding agent Substances 0.000 claims abstract description 8
- 239000005011 phenolic resin Substances 0.000 claims abstract description 7
- 239000000945 filler Substances 0.000 claims abstract description 6
- 238000000465 moulding Methods 0.000 claims abstract description 3
- 239000010425 asbestos Substances 0.000 claims description 4
- 239000003607 modifier Substances 0.000 claims description 4
- 229910052895 riebeckite Inorganic materials 0.000 claims description 4
- 239000012784 inorganic fiber Substances 0.000 claims description 3
- 239000002023 wood Substances 0.000 claims 1
- 150000001463 antimony compounds Chemical class 0.000 abstract description 9
- 150000002611 lead compounds Chemical class 0.000 abstract description 8
- 230000001629 suppression Effects 0.000 abstract description 8
- 238000004321 preservation Methods 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 description 20
- 239000002184 metal Substances 0.000 description 20
- 238000011156 evaluation Methods 0.000 description 10
- 230000007613 environmental effect Effects 0.000 description 8
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 7
- 230000000694 effects Effects 0.000 description 5
- 239000000314 lubricant Substances 0.000 description 5
- 229910052976 metal sulfide Inorganic materials 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000001788 irregular Effects 0.000 description 4
- 230000013011 mating Effects 0.000 description 4
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 230000002159 abnormal effect Effects 0.000 description 3
- 239000004760 aramid Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 244000226021 Anacardium occidentale Species 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 229920003235 aromatic polyamide Polymers 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 235000020226 cashew nut Nutrition 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002905 metal composite material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- RCYJPSGNXVLIBO-UHFFFAOYSA-N sulfanylidenetitanium Chemical compound [S].[Ti] RCYJPSGNXVLIBO-UHFFFAOYSA-N 0.000 description 2
- 150000004763 sulfides Chemical class 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229910001928 zirconium oxide Inorganic materials 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- NNLOHLDVJGPUFR-UHFFFAOYSA-L calcium;3,4,5,6-tetrahydroxy-2-oxohexanoate Chemical compound [Ca+2].OCC(O)C(O)C(O)C(=O)C([O-])=O.OCC(O)C(O)C(O)C(=O)C([O-])=O NNLOHLDVJGPUFR-UHFFFAOYSA-L 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- -1 lead sulfide Chemical class 0.000 description 1
- 229910052981 lead sulfide Inorganic materials 0.000 description 1
- 229940056932 lead sulfide Drugs 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- BFSQJYRFLQUZKX-UHFFFAOYSA-L nickel(ii) iodide Chemical compound I[Ni]I BFSQJYRFLQUZKX-UHFFFAOYSA-L 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- YPMOSINXXHVZIL-UHFFFAOYSA-N sulfanylideneantimony Chemical compound [Sb]=S YPMOSINXXHVZIL-UHFFFAOYSA-N 0.000 description 1
- CADICXFYUNYKGD-UHFFFAOYSA-N sulfanylidenemanganese Chemical compound [Mn]=S CADICXFYUNYKGD-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- AFNRRBXCCXDRPS-UHFFFAOYSA-N tin(ii) sulfide Chemical compound [Sn]=S AFNRRBXCCXDRPS-UHFFFAOYSA-N 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
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- Braking Arrangements (AREA)
Abstract
Description
この発明は、各種ブレーキやクラッチフェーシングなどに利用する摩擦材、特に、環境にやさしく、性能も優れた摩擦材に関する。 The present invention relates to a friction material used for various brakes, clutch facings, and the like, and particularly to a friction material that is environmentally friendly and excellent in performance.
自動車用ブレーキなどに採用される摩擦材(ディスクブレーキ用の摩擦パッドやドラムブレーキ用のブレーキライニングなど)には、従来、耐摩耗性を向上させるために、黒鉛や二硫化モリブデンを配合することが行われている。また、高温域で発生するメタルキャッチによる対面攻撃性の悪化を抑制するために、硫化鉛、酸化アンチモン、硫化アンチモン等の鉛化合物やアンチモン化合物が有効であることが知られている。しかしながら、この鉛化合物やアンチモン化合物は環境問題への取り組みから使用を抑制する動きが高まっている。 Friction materials (such as friction pads for disc brakes and brake linings for drum brakes) used in automobile brakes have conventionally been blended with graphite or molybdenum disulfide to improve wear resistance. Has been done. In addition, it is known that lead compounds and antimony compounds such as lead sulfide, antimony oxide, and antimony sulfide are effective for suppressing the deterioration of the face-to-face attack due to the metal catch generated in a high temperature range. However, there is an increasing trend to suppress the use of lead compounds and antimony compounds due to environmental efforts.
鉛化合物やアンチモン化合物の使用を抑制するためには、環境負荷の小さい代替材料が必要である。そこで、下記特許文献1は、その代替材料として、硫化チタン及び金属複合硫化物以外の金属硫化物を3種以上含有させることを提案しており、含有させる金属硫化物については、硫化亜鉛、硫化銅、硫化ビスマス、硫化錫、硫化鉄、硫化マンガンおよび硫化モリブデンを具体例として挙げている。 In order to suppress the use of lead compounds and antimony compounds, alternative materials with low environmental impact are required. Therefore, Patent Document 1 below proposes that three or more kinds of metal sulfides other than titanium sulfide and metal composite sulfides are contained as an alternative material. For the metal sulfides to be contained, zinc sulfide, sulfide Specific examples include copper, bismuth sulfide, tin sulfide, iron sulfide, manganese sulfide, and molybdenum sulfide.
また、石綿以外の無機質繊維及び/又は無機質粒子5〜70重量%、パラ芳香族ポリアミド系重合体のパルプ状物質5〜70重量%、炭素繊維,カーボンブラック,黒鉛粉末,二硫化モリブデン,二硫化タングステン,窒化硼素,ヨウ化ニッケル,フッ素樹脂よりなる群から選ばれた少なくとも一種の固体潤滑剤1〜30重量%、及び芳香族ポリアミド系繊維2〜50重量%を主たる配合成分とする摩擦材(下記特許文献2参照)や、
金属硫化物である二硫化モリブデンや二硫化タングステンを添加し、さらに、銅、錫、亜鉛、ニッケル、鉄、クロム、モリブデン、タングステンなどの金属を併用した摩擦材(下記特許文献3参照)も開発されている。
Developed friction material (see Patent Document 3 below) that uses metal sulfides such as molybdenum disulfide and tungsten disulfide, and also uses metals such as copper, tin, zinc, nickel, iron, chromium, molybdenum, and tungsten. Has been.
特許文献1は、硫化チタン及び金属複合硫化物以外の金属硫化物を3種以上含有させるとしているが、金属硫化物のみをアンチモン化合物や鉛化合物の代替材として用いるその方法では、メタルキャッチの抑制、摩擦材自身の耐摩耗性、低周波ノイズ(制動時に発生する低周波の異音)の抑制に関して十分に満足できる性能を得ることが難しい。 Patent Document 1 describes that three or more kinds of metal sulfides other than titanium sulfide and metal composite sulfides are contained. However, in the method using only metal sulfides as substitutes for antimony compounds and lead compounds, suppression of metal catch It is difficult to obtain satisfactory performance with respect to wear resistance of the friction material itself and suppression of low frequency noise (low frequency noise generated during braking).
特許文献2の摩擦材も、上記の固体潤滑剤の添加によって温度による摩擦係数の変化が少なく、耐摩耗性に優れ、しかも機械的強度が大きくなると述べているが、その固体潤滑剤の添加量が多すぎるため、(ディスクロータなどの摺動相手材)の表面に生成される被膜が多くなって、ブレーキノイズ(制動時の異音)が発生する。また、潤滑剤過多により、摩擦係数が大幅に低下する。 The friction material of Patent Document 2 also states that the addition of the above-described solid lubricant causes little change in the coefficient of friction due to temperature, has excellent wear resistance, and increases the mechanical strength. Since there are too many, the coating film produced | generated on the surface of (sliding counterpart materials, such as a disc rotor) increases, and brake noise (abnormal noise at the time of braking) generate | occur | produces. In addition, the friction coefficient is significantly reduced due to excessive lubricant.
さらに、特許文献3の摩擦材は、耐熱フェード性および耐水フェード性に優れ、高速、高負荷、降雨等の環境下でも摩擦係数が安定するとされているが、これは焼結金属摩擦材であり、繊維基材、摩擦調整材、充填材などを樹脂の結合材で固めた摩擦材に適用されたものではない。 Furthermore, the friction material of Patent Document 3 has excellent heat and water fade resistance, and is said to have a stable coefficient of friction even in environments such as high speed, high load, and rainfall. This is a sintered metal friction material. The present invention is not applied to a friction material in which a fiber base material, a friction adjusting material, a filler, or the like is hardened with a resin binder.
繊維基材、摩擦調整材、充填材などを樹脂の結合材で固めた摩擦材は、焼結金属摩擦材に比べるとブレーキノイズが少なく、その中でも特に、NAO(Non−asbestos organic)材が日本国内では主流をなしている。 Friction materials made by solidifying fiber base materials, friction modifiers, fillers, etc. with resin binders have less brake noise than sintered metal friction materials, and in particular, NAO (Non-asbestos organic) material is Japan. It is mainstream in Japan.
この発明は、自動車用ブレーキなどに利用されるNAO材に代表される摩擦材について、環境保全の面で好ましくない鉛化合物やアンチモン化合物を使用せずに高温域での耐摩耗性と対面攻撃性の抑制効果を得られるようにすることを課題としている。 The present invention relates to friction materials represented by NAO materials used for automobile brakes and the like, and wear resistance and face-to-face attack at high temperatures without using lead compounds and antimony compounds, which are undesirable in terms of environmental protection. It is an object to be able to obtain an inhibitory effect.
上記の課題を解決するため、この発明においては、硫化タングステンとチタン酸カリウムを併用し、これを、繊維基材、摩擦調整材、充填材、及びバインダーとして添加されるフェノール樹脂を主成分とする原料組成物を成形、硬化してなる摩擦材の原料組成物中に添加した。 In order to solve the above-described problems, in the present invention, tungsten sulfide and potassium titanate are used in combination, and the main component thereof is a fiber base material, a friction modifier, a filler, and a phenol resin added as a binder. The raw material composition was added to the raw material composition of the friction material formed and cured.
チタン酸カリウムは、板状、或いはフレーク状のものに限定されず、ウイスカータイプのものも利用できる。 Potassium titanate is not limited to a plate shape or flake shape, and a whisker type can also be used.
なお、硫化タングステンはその添加量を0.1〜10.0体積%に、また、チタン酸カリウムはその添加量を5.0〜25.0体積%の範囲にそれぞれ収めると好ましい。 Tungsten sulfide is preferably added in an amount of 0.1 to 10.0% by volume, and potassium titanate is preferably added in an amount of 5.0 to 25.0% by volume.
この発明の摩擦材は、鉛化合物やアンチモン化合物の代替材として硫化タングステンとチタン酸カリウムを併用して添加しており、その2者を添加したことによって摺動面にタングステンの酸化物被膜を適量(過多とならい量)生成させることができ、環境問題に配慮しながら所望の耐摩耗性能とメタルキャッチによる対面攻撃性の抑制効果を得ることができる。 In the friction material of the present invention, tungsten sulfide and potassium titanate are used in combination as substitutes for lead compounds and antimony compounds, and by adding these two, an appropriate amount of tungsten oxide film is applied to the sliding surface. It is possible to generate (amount that is excessive), and it is possible to obtain a desired wear resistance performance and an effect of suppressing a face-to-face attack by a metal catch while considering environmental problems.
さらに、メタルキャッチが抑制されることで摺動面各部の不規則な肉厚成長や肉厚減少が抑えられるため、ジャダー(相手材の摺動面の不規則な面変位に起因したジャダー)の抑制も可能になる。 In addition, by suppressing metal catch, irregular thickness growth and thickness reduction of each part of the sliding surface is suppressed, so judder (judder caused by irregular surface displacement of the sliding surface of the mating material) Suppression is also possible.
チタン酸カリウムは硬すぎず、摩擦時に粉砕されるので、低周波のブレーキノイズ(異音)を抑制することも可能である。 Since potassium titanate is not too hard and is pulverized at the time of friction, low-frequency brake noise (abnormal noise) can be suppressed.
また、安定した潤滑性能を得るために従来は潤滑材を数種類組み合わせて使用せざるを得ず、その使用量も多くなりがちであったが、この発明では、低温領域から高温領域まで幅広い潤滑性能を持つ硫化タングステンを使用したので、その添加量を減らすことが可能であり、コストの削減にもつながる。 In addition, in order to obtain stable lubrication performance, it has been conventionally necessary to use several types of lubricants in combination, and the amount used has tended to increase. Since tungsten sulfide having a high concentration is used, the amount of addition can be reduced, leading to cost reduction.
なお、硫化タングステンとチタン酸カリウムの添加量を、上記の好ましいとした範囲に制限した摩擦材は、後述する実施例によって証明されるように、より良い性能を発揮する。 Note that the friction material in which the addition amounts of tungsten sulfide and potassium titanate are limited to the above-described preferable range exhibits better performance as evidenced by examples described later.
以下、この発明の摩擦材の実施の形態について説明する。この発明の摩擦材は、繊維基材として、アラミド繊維、銅繊維などの有機、無機の繊維を使用する。有害な石綿は用いない。また、摩擦調整材及び充填材として、黒鉛、カシューダスト、水酸化カルシウム、マイカ、酸化ジルコニウム、硫酸バリウムなどを使用する。これに加えてこの発明を特徴づけるチタン酸カリウムと硫化タングステンも添加する。 Hereinafter, embodiments of the friction material of the present invention will be described. The friction material of this invention uses organic and inorganic fibers such as aramid fibers and copper fibers as the fiber base material. Do not use harmful asbestos. Further, graphite, cashew dust, calcium hydroxide, mica, zirconium oxide, barium sulfate, etc. are used as the friction modifier and filler. In addition, potassium titanate and tungsten sulfide, which characterize the present invention, are also added.
これらの原料を結合させるバインダー(結合材)は、熱硬化性樹脂、中でも、耐熱性、難燃性、機械的性質などに優れたフェノール樹脂を使用する。そのフェノール樹脂は粉末を添加し、これを一旦溶かして硬化させる。 As a binder (binding material) for bonding these raw materials, a thermosetting resin, especially a phenol resin excellent in heat resistance, flame retardancy, mechanical properties, and the like is used. The phenol resin is added with a powder, which is once dissolved and cured.
このように、硫化タングステンとチタン酸カリウムを併用することで、鉛化合物やアンチモン化合物を用いずにメタルキャッチを減少させることができ、環境問題の解決とメタルキャッチによる対面攻撃性の抑制を同時に実現することが可能になる。 In this way, by using tungsten sulfide and potassium titanate in combination, metal catch can be reduced without using lead compounds and antimony compounds, and simultaneously solving environmental problems and suppressing face-to-face attack by metal catch. It becomes possible to do.
また、メタルキャッチが抑制されることで摺動面各部の不規則な肉厚成長や肉厚減少が抑えられるため、メタルキャッチよる摺動面の面変位によって引き起こされるジャダーも抑制されるようになる。 In addition, since the metal catch is suppressed, irregular thickness growth and thickness reduction of each part of the sliding surface are suppressed, so that judder caused by the surface displacement of the sliding surface by the metal catch is also suppressed. .
このほか、チタン酸カリウムが摩擦時に粉砕されることによって制動時の低周波ノイズ(異音)を抑制することも可能になる。 In addition, low frequency noise (abnormal noise) during braking can be suppressed by pulverizing potassium titanate during friction.
また、低温領域から高温領域まで幅広い潤滑性能を持つ硫化タングステンを使用したことによって潤滑材の添加量を減らすことが可能となり、コストの削減にもつながる。 In addition, the use of tungsten sulfide having a wide range of lubrication performance from a low temperature region to a high temperature region makes it possible to reduce the amount of lubricant added, leading to cost reduction.
なお、硫化タングステンの添加量が0.1体積%未満では、添加の効果が小さくてメタルキャッチの抑制が不十分になる場合があり、そのときには、相手材(例えばディスクロータ)の摩擦面の不規則な肉厚成長や不規則な削れが起こってジャダーを発生させるので、硫化タングステンの添加量は0.1体積%以上にするのがよい。また、この硫化タングステンの添加量が10.0体積%を超えると、酸化被膜が過剰に生成されて相手材に必要以上に付着し、それが原因で低周波ノイズが発生する傾向が高まって実用に適さないものになるので、この硫化タングステンの添加量の上限は10.0体積%にとどめるのがよい。 If the addition amount of tungsten sulfide is less than 0.1% by volume, the effect of addition may be small and the suppression of metal catch may be insufficient. In this case, the friction surface of the counterpart material (for example, the disk rotor) may be insufficient. Since regular wall thickness growth and irregular shaving occur and judder is generated, the addition amount of tungsten sulfide is preferably 0.1% by volume or more. Moreover, if the added amount of tungsten sulfide exceeds 10.0% by volume, an oxide film is excessively formed and adheres to the mating material more than necessary, which increases the tendency to generate low-frequency noise. Therefore, the upper limit of the tungsten sulfide addition amount is preferably limited to 10.0% by volume.
また、併用するチタン酸カリウムは、飛散防止などを考えると、ウイスカータイプのものよりは板状、或いはフレーク状のものが好ましい。 Further, the potassium titanate used in combination is preferably a plate-like or flake-like one rather than a whisker-type one in view of scattering prevention.
このチタン酸カリウムの添加量が5.0体積%未満では、生成された被膜の研削効果(研磨材としての働き)やチタン酸カリウムの自己粉砕による低周波ノイズの抑制効果が小さく、実用性が薄れる。また、そのチタン酸カリウムの添加量が25.0体積%を超えると、被膜の研削効果が大きくなりすぎて相手材の摺動面に適量の酸化物被膜を生成することが難しくなり、所期の耐摩耗性を付与することが難しくなる。また、メタルキャッチの抑制も不十分になり、相手材の摩擦面の肉厚差が成長してジャダーの発生が考えられるようになる。 When the added amount of potassium titanate is less than 5.0% by volume, the grinding effect of the produced coating (working as an abrasive) and the low frequency noise suppression effect due to self-grinding of potassium titanate are small and practical. Fade. On the other hand, if the amount of potassium titanate exceeds 25.0% by volume, the grinding effect of the coating becomes too great, and it becomes difficult to form an appropriate amount of oxide coating on the sliding surface of the counterpart material. It becomes difficult to impart the wear resistance. Moreover, the suppression of the metal catch becomes insufficient, and the difference in the thickness of the friction surface of the mating material grows, and the occurrence of judder can be considered.
なお、この発明の摩擦材は、必要な原料を所定の比率で混合して得られる原料組成物を、所定の温度と圧力を加えて成形し、さらに、バインダーのフェノール樹脂を熱硬化させ、必要に応じて仕上げ研磨などを施して摩擦パッドなどの所望の製品に仕上げる。成形と硬化は、特許文献1が開示しているような方法や摩擦材製造の一般的な方法で行える。製造条件も、特別な条件は必要でなく、特許文献1が開示しているような条件で足りる。 The friction material of the present invention is formed by forming a raw material composition obtained by mixing necessary raw materials at a predetermined ratio by applying predetermined temperature and pressure, and further thermosetting the phenol resin of the binder. Depending on the condition, finish polishing or the like is performed to obtain a desired product such as a friction pad. Molding and curing can be performed by a method as disclosed in Patent Document 1 or a general method for manufacturing a friction material. As for the manufacturing conditions, no special conditions are required, and the conditions disclosed in Patent Document 1 are sufficient.
−実施例−
性能評価のための摩擦材を製造した。その摩擦材の原料成分とその原料成分の含有量を表1に示す。表1の実施例1〜23は発明品、比較例1〜5は比較品である。発明品と比較品は、繊維基材、黒鉛、カシューダスト、水酸化カルシウム、マイカ、酸化ジルコニウム及びバインダーの粉末フェノール樹脂の含有量を同じにし、他の添加成分とその添加量を異ならせた。
-Example-
A friction material for performance evaluation was manufactured. Table 1 shows the raw material components of the friction material and the contents of the raw material components. Examples 1 to 23 in Table 1 are invention products, and Comparative Examples 1 to 5 are comparative products. Inventive products and comparative products were made to have the same powder phenolic resin content of fiber base material, graphite, cashew dust, calcium hydroxide, mica, zirconium oxide, and binder, and the additive amount was different from other additive components.
性能評価の試験結果を表2に示す。性能評価は、温度別摩耗試験を行い、その摩耗試験におけるメタルキャッチの発生状況と、低周波ノイズの発生状況、環境負荷への影響について調べた。試験の方法と評価の基準を以下にまとめる。 Table 2 shows the test results of the performance evaluation. For performance evaluation, we conducted a wear test for each temperature, and investigated the occurrence of metal catches, the occurrence of low-frequency noise, and the impact on the environmental load. The test methods and evaluation criteria are summarized below.
・〔摩耗試験〕
制動初速度50km/h、制動減速度0.3G、制動回数1000回換算、制動前温度100℃、200℃、300℃、400℃の条件での摩耗量を測定。
・〔メタルキャッチの発生〕
上記の摩耗試験において、各温度の摩耗量測定時にメタルキャッチの発生状況を観察し、下記基準で評価。
◎:メタルキャッチ無し。○:長径3mm以下の小さなメタルキャッチ数個以下。
△:小さなメタルキャッチ多数。×:長径5mm以上の大きなメタルキャッチ。
・〔平均摩擦係数〕
JASO C406 の第2効力時の摩擦係数の平均値
・〔低周波ノイズ〕
実車評価で時速40km/h、制動前ブレーキ温度60℃、90℃、120℃、150℃、180℃、150℃、120℃、90℃、60℃、制動減速度0.2G、0.3G、0.4G、0.6G、0.8Gにおいて、ドライバーの官能評価で2kHz以下の低周波ノイズの音圧が大レベル発生時×、中レベル発生時△、小レベル発生時○、発生無し◎。
・〔肉厚差成長〕
相手材であるディスクロータの摩擦面の肉厚を測定し、測定値の最大値と最小値の差を算出。
・〔環境負荷〕
原料組成物中にアンチモン化合物をごく少量でも含むものは環境負荷への影響×、全く含んでいないもののみ◎。ウイスカー状のチタン酸カリウムは、作業環境内での飛散が考えられるので△とした。
・ [Abrasion test]
Measures the amount of wear under conditions of braking initial speed 50 km / h, braking deceleration 0.3 G, braking count 1000 conversion, pre-braking temperature 100 ° C, 200 ° C, 300 ° C, 400 ° C.
・ [Generation of metal catches]
In the above wear test, the occurrence of metal catch was observed when measuring the amount of wear at each temperature, and evaluated according to the following criteria.
A: No metal catch. ○: Several small metal catches with a major axis of 3 mm or less.
Δ: Many small metal catches. X: A large metal catch having a major axis of 5 mm or more.
・ [Average friction coefficient]
Average value of coefficient of friction at the time of the second effect of JASO C406 ・ [Low frequency noise]
40km / h in actual vehicle evaluation, brake temperature before braking 60 ° C, 90 ° C, 120 ° C, 150 ° C, 180 ° C, 150 ° C, 120 ° C, 90 ° C, 60 ° C, braking deceleration 0.2G, 0.3G, At 0.4G, 0.6G, and 0.8G, the sound pressure of low frequency noise of 2 kHz or less when the driver's sensory evaluation is large level x, medium level generation Δ, small level generation ○, no generation ◎.
・ [Thickness difference growth]
Measure the thickness of the friction surface of the disk rotor that is the mating material, and calculate the difference between the maximum and minimum values.
·〔Environmental load〕
If the raw material composition contains an antimony compound even in a very small amount, the impact on the environmental impact is X. Since whisker-like potassium titanate is considered to be scattered in the work environment, it was evaluated as Δ.
−評価−
表2からわかるように、発明品の中でも、硫化タングステンの添加量を0.1〜10.0体積%、チタン酸カリウムの添加量を5.0〜25.0体積%にした実施例4〜6,9〜14,および17〜19は、全ての評価項目において×の評価が無く、総合的に判断して良好な結果が得られている。発明品の中でも特に実施例4,実施例10〜12および実施例18は、すべての評価項目が○と◎になっている上に肉厚差成長も小さく、これらの成分配合率での実施が推奨される。
-Evaluation-
As can be seen from Table 2, among the invention products, Examples 4 to 4 in which the addition amount of tungsten sulfide was 0.1 to 10.0% by volume and the addition amount of potassium titanate was 5.0 to 25.0% by volume. In the evaluation items 6, 9 to 14, and 17 to 19, there is no evaluation of x in all the evaluation items, and good results are obtained by comprehensive judgment. Among the inventive products, in particular, Examples 4, Examples 10 to 12, and Example 18 have all evaluation items as ◯ and ◎, and also have small thickness difference growth. Recommended.
なお、この発明の摩擦材は、ディスクロータやドラムロータを相手材とするディスクブレーキ用の摩擦パッドやドラムブレーキ用のブレーキシューなどに利用するのに適しているが、クラッチフェーシングなどにも利用できる。 The friction material of the present invention is suitable for use as a disk brake friction pad or a drum brake brake shoe with a disk rotor or drum rotor as a counterpart material, but it can also be used for clutch facing and the like. .
Claims (3)
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014104125A1 (en) * | 2012-12-25 | 2014-07-03 | 株式会社アドヴィックス | Friction material and method for producing same |
| WO2014185307A1 (en) * | 2013-05-15 | 2014-11-20 | 大塚化学株式会社 | Friction material and friction material for use in drum brake |
| JP2018053254A (en) * | 2017-10-25 | 2018-04-05 | 日立化成株式会社 | Non-asbestos friction material composition |
| JP2020117726A (en) * | 2020-04-09 | 2020-08-06 | 日立化成株式会社 | Friction material and friction member |
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2007
- 2007-02-05 JP JP2007025128A patent/JP2008189791A/en active Pending
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014104125A1 (en) * | 2012-12-25 | 2014-07-03 | 株式会社アドヴィックス | Friction material and method for producing same |
| WO2014185307A1 (en) * | 2013-05-15 | 2014-11-20 | 大塚化学株式会社 | Friction material and friction material for use in drum brake |
| JP2014224175A (en) * | 2013-05-15 | 2014-12-04 | 大塚化学株式会社 | Friction material and friction material for use in drum brake |
| JP2018053254A (en) * | 2017-10-25 | 2018-04-05 | 日立化成株式会社 | Non-asbestos friction material composition |
| JP2020117726A (en) * | 2020-04-09 | 2020-08-06 | 日立化成株式会社 | Friction material and friction member |
| JP7020506B2 (en) | 2020-04-09 | 2022-02-16 | 昭和電工マテリアルズ株式会社 | Friction materials and friction members |
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